基于3S技术对太湖底质及水质总磷的研究

应用3S技术研究了太湖底质与水质总磷(TP)的分布情况,并结合水华频次分析了其相关性。结果表明:2016—2018年,太湖底质TP年均值在433~537 mg/kg波动,水质TP年均值从0.064 mg/L上升至0.087 mg/L。从空间分布来看,底质TP、水质TP和水华频次均呈现“西高东低”的规律,太湖西部区尤其是竺山湖区是需要开展治理的重点区域。3年间,太湖西部区水质TP上升,而底质TP与入湖河流TP下降,说明内源磷污染是太湖西部区水质TP升高的主要原因,须加强科学清淤。     

Temporal and Spatial Trends in Nutrient and Sediment Loading to Lake Tahoe,California‐Nevada,USA

Since 1980, the Lake Tahoe Interagency Monitoring Program (LTIMP) has provided stream‐discharge and water quality data—nitrogen (N), phosphorus (P), and suspended sediment—at more than 20 stations in Lake Tahoe Basin streams. To characterize the temporal and spatial patterns in nutrient and sediment loading to the lake, and improve the usefulness of the program and the existing database, we have (1) identified and corrected for sources of bias in the water quality database; (2) generated synthetic datasets for sediments and nutrients, and resampled to compare the accuracy and precision of different load calculation models; (3) using the best models, recalculated total annual loads over the period of record; (4) regressed total loads against total annual and annual maximum daily discharge, and tested for time trends in the residuals; (5) compared loads for different forms of N and P; and (6) tested constituent loads against land use‐land cover (LULC) variables using multiple regression. The results show (1) N and P loads are dominated by organic N and particulate P; (2) there are significant long‐term downward trends in some constituent loads of some streams; and (3) anthropogenic impervious surface is the most important LULC variable influencing water quality in basin streams. Many of our recommendations for changes in water quality monitoring and load calculation methods have been adopted by the LTIMP.     

Implications of Conceptual Channel Representation on SWAT Streamflow and Sediment Modeling

Hydrologic modeling outputs are influenced by how a watershed system is represented. Channel routing is a typical example of the mathematical conceptualization of watershed landscape and processes in hydrologic modeling. We investigated the sensitivity of accuracy, equifinality, and uncertainty of Soil and Water Assessment Tool (SWAT) modeling to channel dimensions to demonstrate how a conceptual representation of a watershed system affects streamflow and sediment modeling. Results showed the amount of uncertainty and equifinality strongly responded to channel dimensions. On the other hand, the model performance did not significantly vary with the changes in the channel representation due to the degree of freedom allowed by the conceptual nature of hydrologic modeling in the parameter calibration. Such findings demonstrated good modeling performance statistics do not necessarily mean small output uncertainty, and partial improvements in the watershed representation may neither increase modeling accuracy nor reduce uncertainty. We also showed the equifinality and uncertainty of hydrologic modeling are case‐dependent rather than specific to models or regions, suggesting great caution should be used when attempting to transfer uncertainty analysis results to other modeling studies, especially for ungauged watersheds. Editor's note: This paper is part of the featured series on SWAT Applications for Emerging Hydrologic and Water Quality Challenges. See the February 2017 issue for the introduction and background to the series.     

Forensic Evaluation of Metals (Cr,Cu, Pb,Zn), Isotopes (δ13C and δ15N), and C:N Ratios in Freshwater Sediment

A forensic approach was used to evaluate sediments from Portão Stream, including analysis of metals, carbon (C) and nitrogen (N) stable isotopes, and C:N ratios. Samples collected at various points located along the stream were tested in order to investigate a possible illegal leachate input. The studied stream is heavily impacted by sewage and industrial discharges from two cities along its course. Among the metals analyzed, chromium (Cr) was noticeably the main pollutant, showing the highest levels, above regulatory limits, downstream from some potential sources of effluents enriched with this metal. Isotope analyses revealed a general trend of depletion in the heavier isotope along the stream for C and N. The exception was one point near a hazardous waste landfill, where relatively more enriched δ¹³C and δ¹⁵N values were found. The isotope and metal analysis results indicated that this site was affected by a particular source, demonstrating the combination of these parameters could be used for the discrimination of sources in a heavily polluted stream. Nevertheless, further investigations are necessary to provide a comprehensive evaluation of the biogeochemical processes involved in the incorporation of leachate in sediments to use this analysis as evidence for the illegal leachate discharge.     

Concentrations and distributions of 18 organochlorine pesticides listed in the Stockholm Convention in surface sediments from the Liaohe River basin,China

Organochlorine pesticides (OCPs) were analyzed in 26 surface sediment samples from the Liaohe River basin, and the distributions of and potential environmental risks posed by OCPs in the basin were evaluated. Eighteen OCPs listed in the Stockholm Convention were determined using isotope-dilution gas chromatography–high resolution mass spectrometry. This is the first study of hexachlorobenzene (HCB) in the Liaohe River basin sediments. The total OCP concentrations were 0.39–68.06 ng g^?1 dry weight. The total α-, β-, γ-, and δ-hexachlorocyclohexane (HCH), the total dichlorodiphenyltrichloroethane (DDT – p,p′-dichlorodiphenyldichloroethane (DDD), p,p′-dichlorodiphenyldichloroethylene (DDE), o,p^'-DDT, and p,p′-DDT), and the HCB concentrations in the sediment samples were 0.1–28.48 ng g^?1 (mean 4.01 ng g^?1), 0.08–6.52 ng g^?1 (mean 3.07 ng g^?1), and 0.18–24.8 ng g^?1 (mean 4.38 ng g^?1), respectively. The HCB concentrations were higher than the concentrations of the other OCPs, and the HCHs and HCB together were the dominant OCPs. β-HCH was the most abundant HCH isomer. The concentrations of DDTs and other OCPs were relatively low, and the (DDE+DDD)/DDT ratios (>0.5) and DDD/DDE ratios (<1) indicated that no recent DDT inputs had occurred in the Liaohe River system. The main sources of HCHs were probably the historical production and agricultural use of HCH in the study area. The DDT and HCH concentrations were generally below or similar to the concentrations that have been found in other parts of the world. An ecotoxicological evaluation indicated that HCHs in surface sediments pose slight risks to human and ecological health in the Liaohe River basin.     

应用相平衡分配法建立湘江衡阳段沉积物重金属质量基准

采集湘江衡阳段29个站点的表层沉积物样品,测定沉积物中4种重金属(Cu、Pb、Zn和Cd)含量及赋存形态、以及孔隙水中重金属含量,根据相平衡分配法的基本理论,考虑参与沉积物-水相平衡分配的重金属组成,实测法计算重金属的沉积物-水相平衡分配系数(Kp),分别引用美国EPA制定保护水生生物不受重金属慢性毒性影响的基本连续浓度(CCC)和我国地表水环境质量标准(GB 3838-2002)Ⅰ类水质标准,建立两种湘江衡阳段沉积物重金属质量基准(SQC)进行对比分析,其中基于美国CCC建立的湘江衡阳段沉积物重金属质量基准与国内外研究成果相比可比性较好,4种重金属(Cu、Pb、Zn和Cd)的SQC值分别为64.62、55.57、1 360.40和2.34μg.g-1,此SQC具有保护长期生活于沉积物中的底栖生物不受重金属慢性毒性影响的意义.通过单因子评价法将湘江衡阳段沉积物中重金属总量与沉积物质量基准值(SQC)进行比较,结果表明,湘江衡阳段沉积物中Cd和Pb含量水平对底栖生物具有较大的慢性毒性影响,Cd污染不容忽视.     

西大海湖沉积物营养盐垂直分布特征变化分析

通过对西大海湖心柱状沉积岩芯有机质(OM)、总氮(TN)、总磷(TP)、磷形态和粒度指标的测试和分析,探讨其垂向分布特征及影响因素.结果表明,营养盐中OM、TN和TP的含量分别为0.633%~2.756%、0.150%~0.429%和648.00~1 480.67 mg·kg-1.Ca-P是TP的主要部分,占TP含量66.04%.1843~1970年间,Ca-P、IP、OM含量变化较小,Fe/Al-P、OP、TP、TN含量波动较大;1970~1996年间,Ca-P、IP、TP含量变化均呈减小趋势,Fe/Al-P、OP、OM含量不同程度上先减少后增加,TN波动较大;1996~2009年营养元素含量相对波动较大,Fe/Al-P、OP和OM的平均含量是3个阶段中最高的.西大海湖沉积岩芯营养元素污染来源以工业废水、生活污水和化肥农药的流失为主.沉积物中C/N比值显示有机质主要来源于水生生物.沉积物粒度组成以黏土和细粉砂为主.相关性研究表明,Ca-P、IP与TP均呈显著的正相关关系,表明Ca-P对IP、TP的增长贡献大.     

太湖表层水体及沉积物中双酚A类似物的分布特征及潜在风险

本研究对太湖表层水和沉积物中7种双酚A类似物(BPs)的浓度水平及分布特征进行了调查,并对其潜在的风险进行了评估.结果表明太湖表层水中双酚F(BPF)、双酚S(BPS)和双酚A(BPA)为主要的BPs组分;沉积物中BPA对BPs总浓度的贡献率最高,其次为BPF和BPS,且与沉积物中TOC含量具有显著的正相关;BPA、BPF和BPS在表层水和沉积物中的高浓度水平均分布在太湖入湖支流(采样点S4~S10).风险评估表明BPs的联合毒性风险熵表现出低生态风险,且对人体不具有明显的健康风险.     

覆盖金属氧化物对湖泊沉积物溶解性有机质特征的影响

为揭示不同金属氧化物对湖泊沉积物DOM（溶解性有机质）影响机制,通过室内模拟试验,在沉积物表层分别覆盖Fe、Al、Mn氧化物及湖沙后培养1 a,并利用三维荧光和紫外光谱方法进行表征.结果表明:① 覆盖Al、Fe、Mn氧化物和湖沙主要降低了0~3 cm沉积物的w（DOC）,降幅分别为8.61%、6.27%、22.38%和0.44%. ② 沉积物中DOM的类络氨酸峰（peak B₁）和类色氨酸峰（peak T₂）均产生较大变化.其中三种氧化物均显著降低了上层沉积物中DOM的peak T₂,使底层DOM的peakT₂显著增加. Mn氧化物使DOM的peak B₁降低,Fe和Al氧化物使DOM的peak B₁增加,湖沙则使两类峰均降低. ③ 覆盖金属氧化物改变了沉积物DOM结构特征,其中覆盖Fe氧化物增强了其芳香性,而覆盖Mn氧化物和Al氧化却降低其芳香性,但三者均使DOM腐质化程度及官能团数量增加,并使FI（Fluorescence Index,荧光指数）增大,表明DOM向生物源转化.研究显示,沉积物表层覆盖金属氧化物影响了沉积物中DOM迁移和转化,并促进了其降解,导致其分子量和腐殖化程度增加.      

大冶湖表层水和沉积物中重金属污染特征与风险评价

于2014年4月采集大冶湖表层水和表层沉积物,用原子吸收分光光度法测定其重金属含量,并基于健康风险评价模型和潜在生态风险指数法开展表层水和沉积物重金属污染的潜在健康风险和生态风险评价.结果表明,表层水和沉积物重金属(Ni、Cd、Cu和Pb)含量平均值分别为49.27、2.19、12.18、12.13μg·L~(-1)和78.46、77.13、650.13、134.22 mg·kg~(-1).富集系数显示,Cd、Cu和Pb均为重度富集,尤其是Cd累积最为明显.与国内典型湖泊重金属污染相比,表层水和沉积物中重金属元素含量均相对较高.表层水和沉积物重金属元素均表现为湖湾处含量较高,中部含量较均匀的分布规律,其来源主要受多种人为活动污染.环境风险评价显示,重金属类化学物质通过饮水途径产生健康风险范围为9.77E-08~1.63E-05 a-1,Ni和Cd是水环境健康风险的优先管理对象.沉积物重金属的潜在生态风险高低为CdCuPbNi,其中Cd是生态风险的贡献元素.